Canonical Allele Identifier: CA1703635031
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147966G= , CM000669.2:g.44147966G= GRCh38
NC_000007.13:g.44187565G= , CM000669.1:g.44187565G= GRCh37
NC_000007.12:g.44154090G= NCBI36
NG_008847.1:g.46458C=
NG_008847.2:g.55205C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*678-133C= ENSP00000379142.4:n.*678-133C=
ENST00000616242.5:c.680-133C= ENSP00000482149.2:n.680-133C=
ENST00000345378.7:c.683-133C= ENSP00000223366.2:n.683-133C=
ENST00000403799.8:c.680-133C= MANE Select ENSP00000384247.3:n.680-133C=
ENST00000671824.1:c.680-133C= ENSP00000500264.1:n.680-133C=
ENST00000673284.1:c.680-133C= ENSP00000499852.1:n.680-133C=
ENST00000345378.6:c.683-133C= ENSP00000223366.2:n.683-133C=
ENST00000395796.7:c.677-133C= ENSP00000379142.3:n.677-133C=
ENST00000403799.7:c.680-133C= ENSP00000384247.3:n.680-133C=
ENST00000437084.1:c.629-133C= ENSP00000402840.1:n.629-133C=
ENST00000616242.4:c.677-133C= ENSP00000482149.1:n.677-133C=
NM_000162.3:c.680-133C= NP_000153.1:n.680-133C=
NM_033507.1:c.683-133C= NP_277042.1:n.683-133C=
NM_033508.1:c.677-133C= NP_277043.1:n.677-133C=
XR_927223.1:n.82+218G=
NM_000162.4:c.680-133C= NP_000153.1:n.680-133C=
NM_001354800.1:c.680-133C= NP_001341729.1:n.680-133C=
NM_033507.2:c.683-133C= NP_277042.1:n.683-133C=
NM_033508.2:c.677-133C= NP_277043.1:n.677-133C=
XR_927223.2:n.82+218G=
NM_000162.5:c.680-133C= MANE Select NP_000153.1:n.680-133C=
NM_033507.3:c.683-133C= NP_277042.1:n.683-133C=
NM_033508.3:c.677-133C= NP_277043.1:n.677-133C=